Clinical trial Recruiting at 1 site Interventional Ages 18 to 80

How different foods change blood sugar after a meal.

Official title: Quantifying Differential Individual Responses to OGTT, Starchy Foods, and Mitigators and Its Association With Metabolic Subphenotypes

Run by Stanford University · NCT06989164 · Data updated 2026-11-12

This project will test whether adding things like fiber, vinegar, amino acids, protein, or exercise to a standard meal changes post-meal blood sugar in people with prediabetes, type 2 diabetes, and healthy adults.

Quick facts

Study typeInterventional
Ages18 Years to 80 Years
SexAll
Enrollment100 (estimated)
SponsorStanford University
Academic / other
Locations1 site (Stanford, California)
StatusRecruiting
StartedOctober 1, 2025
Main results expectedNovember 30, 2028
Study endsNovember 30, 2028
Registry record updatedDecember 2, 2025
Trial IDNCT06989164 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults with BMI between 19 and 45 kg/m2, HbA1c ≤7.0% who are not taking antihyperglycemic medications and who can come to Stanford for on-site metabolic testing (including people with prediabetes, type 2 diabetes, or healthy controls).

Probably not a fit

People with recent cardiovascular events, active cancer, kidney or liver disease, pregnancy or lactation, chronic inflammatory disease, eating disorders, prior bariatric surgery, current use of diabetes or weight-loss medications, heavy alcohol use, or who cannot travel to Stanford are unlikely to benefit from participation.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

Participants will wear a continuous glucose monitor and eat pre-measured cooked rice on separate test days while investigators add potential mitigators (fiber, acid/vinegar, an amino acid such as leucine, whole protein, or exercise) to each meal. Some visits will include finger‑stick blood microsamples and saliva collected before and after the test meal, and a baseline stool sample will be collected once. Each condition is tested on a different day with standardized instructions to compare individual postprandial glucose responses. The goal is to identify patterns of metabolism that predict which simple dietary or behavioral changes best blunt glucose spikes for different people.

Why it matters

Potential benefit: If successful, this work could enable personalized food or behavior recommendations to reduce post-meal blood sugar spikes for individuals.

How similar studies have gone: Previous research has shown large individual differences in post-meal glucose responses and that interventions like fiber, protein, or vinegar can blunt spikes, but this study applies multiple mitigators in a standardized protocol to better characterize which approaches work for which people.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* BMI (body mass index) \>19 kg/m2 but \< 45 kg/m2
* HbA1c \< or equal to 7.0% while not on antihyperglycemic medications
* Be willing to provide written informed consent for all study procedures.
* Able to commute to Stanford campus for on-site visits

Exclusion Criteria:

* recent (\<6mos) CVD (cardiovascular disease) event
* active malignancy
* kidney/liver disease
* pregnancy/lactation
* chronic inflammatory disease
* eating disorder
* bariatric surgery
* history of acute pancreatitis
* current use of antihyperglycemic, diabetogenic, or weight loss medications
* heavy alcohol use
* physical activity \>2 hours/day
* inability to come to Stanford CTRU (Clinical and Translational Research Unit) for metabolic testing

Where it's running

  • Stanford University
    Stanford, California, United States
    Recruiting

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.